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Ron A Wevers

Showing results (171-180 of 266) with videos related to

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Diabetologia|April 7, 2017
SUCNR1-mediated chemotaxis of macrophages aggravates obesity-induced inflammation and diabetesJanna A van Diepen, Joris H Robben, Guido J Hooiveld, et al.
Pediatrics|September 12, 2012
Defining the phenotype in congenital disorder of glycosylation due to ALG1 mutationsEva Morava, Julia Vodopiutz, Dirk J Lefeber, et al.
Journal of Inherited Metabolic Disease|January 25, 2018
The role of the clinician in the multi-omics era: are you ready?Clara D M van Karnebeek, Saskia B Wortmann, Maja Tarailo-Graovac, et al.
NMR in Biomedicine|March 17, 2009
Guanidinoacetate methyltransferase (GAMT) deficiency diagnosed by proton NMR spectroscopy of body fluidsUdo F H Engelke, Maria Tassini, Joseph Hayek, et al.
NMR in Biomedicine|February 27, 2010
Silent increase of urinary ethylmalonic acid is an indicator of nonspecific brain dysfunctionRaffaella Zannolli, Sabrina Buoni, Maria Tassini, et al.
European Journal of Human Genetics : EJHG|February 5, 2015
Truncated prelamin A expression in HGPS-like patients: a transcriptional studyFlorian Barthélémy, Claire Navarro, Racha Fayek, et al.
Blood|July 3, 2014
Characterization of acute myeloid leukemia based on levels of global hydroxymethylationLeonie I Kroeze, Mariam G Aslanyan, Arno van Rooij, et al.
The European Respiratory Journal|May 28, 2016
Hydrogen cyanide emission in the lung by Staphylococcus aureusAnne H Neerincx, Ylona A M Linders, Laura Vermeulen, et al.
Annals of Neurology|June 27, 2009
Free sialic acid storage disease without sialuriaFanny Mochel, Bingzhi Yang, Julie Barritault, et al.
Annals of Neurology|October 31, 2012
DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsyRita Barone, Chiara Aiello, Valérie Race, et al.
Pageof 27

Showing results (171-180 of 266) with videos related to

Sort By:
Pageof 27
Diabetologia|April 7, 2017
SUCNR1-mediated chemotaxis of macrophages aggravates obesity-induced inflammation and diabetesJanna A van Diepen, Joris H Robben, Guido J Hooiveld, et al.
Pediatrics|September 12, 2012
Defining the phenotype in congenital disorder of glycosylation due to ALG1 mutationsEva Morava, Julia Vodopiutz, Dirk J Lefeber, et al.
Journal of Inherited Metabolic Disease|January 25, 2018
The role of the clinician in the multi-omics era: are you ready?Clara D M van Karnebeek, Saskia B Wortmann, Maja Tarailo-Graovac, et al.
NMR in Biomedicine|March 17, 2009
Guanidinoacetate methyltransferase (GAMT) deficiency diagnosed by proton NMR spectroscopy of body fluidsUdo F H Engelke, Maria Tassini, Joseph Hayek, et al.
NMR in Biomedicine|February 27, 2010
Silent increase of urinary ethylmalonic acid is an indicator of nonspecific brain dysfunctionRaffaella Zannolli, Sabrina Buoni, Maria Tassini, et al.
European Journal of Human Genetics : EJHG|February 5, 2015
Truncated prelamin A expression in HGPS-like patients: a transcriptional studyFlorian Barthélémy, Claire Navarro, Racha Fayek, et al.
Blood|July 3, 2014
Characterization of acute myeloid leukemia based on levels of global hydroxymethylationLeonie I Kroeze, Mariam G Aslanyan, Arno van Rooij, et al.
The European Respiratory Journal|May 28, 2016
Hydrogen cyanide emission in the lung by Staphylococcus aureusAnne H Neerincx, Ylona A M Linders, Laura Vermeulen, et al.
Annals of Neurology|June 27, 2009
Free sialic acid storage disease without sialuriaFanny Mochel, Bingzhi Yang, Julie Barritault, et al.
Annals of Neurology|October 31, 2012
DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsyRita Barone, Chiara Aiello, Valérie Race, et al.
Pageof 27